Evidence map›Paper›PMID 33035747›Full record

ArticleRespiratory medicine2020

Combining biomarkers of clot resolution and alveolar basement membrane destruction predicts mortality in the ECLIPSE COPD cohort.

Jannie M B Sand, Sarah R Rønnow, Lasse L Langholm, Morten A Karsdal, Tina Manon-Jensen, Ruth Tal-Singer, Bruce E Miller, Jørgen Vestbo, Diana J Leeming

Open access · bronzeAbstract read
In one paragraph

Article in Respiratory medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.4field-weighted citation impact, top 33% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 4 citations in OpenAlex.

  1. Hallmarks of the ageing lung: 10 years later.The European respiratory journal · 2026
    Review
  2. Article
  3. Pathological remodeling of distal lung matrix in end-stage cystic fibrosis patients.Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society · 2022
    Article
  4. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 4 institutions in 3 countries.

Jannie M B SandNordic Bioscience A/S, Herlev, Denmark. Electronic address: jsa@nordicbio.com.
Sarah R RønnowNordic Bioscience A/S, Herlev, Denmark; University of Southern Denmark, The Faculty of Health Science, Odense, Denmark.
Lasse L LangholmNordic Bioscience A/S, Herlev, Denmark.
Morten A KarsdalNordic Bioscience A/S, Herlev, Denmark.
Tina Manon-JensenNordic Bioscience A/S, Herlev, Denmark.
Ruth Tal-SingerGSK R&D, Collegeville, PA, USA.
Bruce E MillerGSK R&D, Collegeville, PA, USA.
Jørgen VestboDivision of Infection Immunity and Respiratory Medicine, University of Manchester, Manchester, UK.
Diana J LeemingNordic Bioscience A/S, Herlev, Denmark.
Nordic Bioscience (Denmark) · DKGlaxoSmithKline (United States) · USUniversity of Manchester · GBUniversity of Southern Denmark · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundChronic obstructive pulmonary disease (COPD) is characterized by abnormal epithelial repair resulting in a hypercoagulable state with intra-alveolar accumulation of fibrin and alveolar basement membrane destruction. This study aimed to investigate if the combination of two serological biomarkers evaluating these pathological processes could improve the prediction of mortality risk compared to single biomarkers.

methodsMatrix metalloproteinase-mediated degradation of the type IV collagen α3 chain (C4Ma3), located in the alveolar basement membrane, and plasmin-mediated degradation of crosslinked fibrin (X-FIB), an end-product of fibrinogen, were assessed serologically in a subset of the ECLIPSE cohort (n = 982). Biomarker data were dichotomized into high versus low at the median. Cox regression and Kaplan-Meier curves were used to analyze the predictive value of having one or two high biomarkers for all-cause mortality over two years.

resultsCOPD participants with high levels of two biomarkers were at significantly higher risk of all-cause mortality with a hazard ratio of 7.66 (95% CI 1.75-33.48; p = 0.007) while participants with one high biomarker were not at significantly higher risk (HR 3.79 [95% CI 0.85-16.94]; p = 0.08).

conclusionsA combination of serological biomarkers of alveolar basement membrane destruction and clot resolution was predictive of all-cause mortality in COPD. The combination of two different pathological aspects may strengthen prognostic accuracy and could be used in conjunction with clinical assessment to guide treatment decisions.

Indexed as

AgedAutoantigensBasement MembraneBiomarkersCause of DeathCohort StudiesCollagen Type IVFemaleForecastingHumansMaleMiddle AgedPredictive Value of TestsPrognosisPulmonary AlveoliPulmonary Disease, Chronic ObstructiveAutoantigensBiomarkersCollagen Type IVtype IV collagen alpha3 chainBasement membraneBiomarkersClot resolutionCOPDFibrinogenMortality

Identifiers

PMID33035747
PMCPMC7530580
OpenAlexW3090705755

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.